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• • A—HUMAN NECESSITIES
  • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
  • A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
  • A61K31/00—Medicinal preparations containing organic active ingredients
  • A61K31/33—Heterocyclic compounds
  • A61K31/395—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins
  • A61K31/435—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having six-membered rings with one nitrogen as the only ring hetero atom
  • A61K31/4353—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having six-membered rings with one nitrogen as the only ring hetero atom ortho- or peri-condensed with heterocyclic ring systems
  • A61K31/4355—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having six-membered rings with one nitrogen as the only ring hetero atom ortho- or peri-condensed with heterocyclic ring systems the heterocyclic ring system containing a five-membered ring having oxygen as a ring hetero atom
• • A—HUMAN NECESSITIES
  • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
  • A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
  • A61K31/00—Medicinal preparations containing organic active ingredients
  • A61K31/33—Heterocyclic compounds
  • A61K31/395—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins
  • A61K31/435—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having six-membered rings with one nitrogen as the only ring hetero atom
  • A61K31/4353—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having six-membered rings with one nitrogen as the only ring hetero atom ortho- or peri-condensed with heterocyclic ring systems
  • A61K31/436—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having six-membered rings with one nitrogen as the only ring hetero atom ortho- or peri-condensed with heterocyclic ring systems the heterocyclic ring system containing a six-membered ring having oxygen as a ring hetero atom, e.g. rapamycin
• • A—HUMAN NECESSITIES
  • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
  • A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
  • A61K45/00—Medicinal preparations containing active ingredients not provided for in groups A61K31/00 - A61K41/00
  • A61K45/06—Mixtures of active ingredients without chemical characterisation, e.g. antiphlogistics and cardiaca
• • A—HUMAN NECESSITIES
  • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
  • A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
  • A61P11/00—Drugs for disorders of the respiratory system
• • A—HUMAN NECESSITIES
  • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
  • A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
  • A61P11/00—Drugs for disorders of the respiratory system
  • A61P11/06—Antiasthmatics
• • A—HUMAN NECESSITIES
  • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
  • A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
  • A61P43/00—Drugs for specific purposes, not provided for in groups A61P1/00-A61P41/00
• • A—HUMAN NECESSITIES
  • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
  • A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
  • A61P7/00—Drugs for disorders of the blood or the extracellular fluid
  • A61P7/02—Antithrombotic agents; Anticoagulants; Platelet aggregation inhibitors
• • A—HUMAN NECESSITIES
  • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
  • A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
  • A61P9/00—Drugs for disorders of the cardiovascular system
• • A—HUMAN NECESSITIES
  • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
  • A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
  • A61P9/00—Drugs for disorders of the cardiovascular system
  • A61P9/04—Inotropic agents, i.e. stimulants of cardiac contraction; Drugs for heart failure
• • A—HUMAN NECESSITIES
  • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
  • A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
  • A61P9/00—Drugs for disorders of the cardiovascular system
  • A61P9/10—Drugs for disorders of the cardiovascular system for treating ischaemic or atherosclerotic diseases, e.g. antianginal drugs, coronary vasodilators, drugs for myocardial infarction, retinopathy, cerebrovascula insufficiency, renal arteriosclerosis
• • A—HUMAN NECESSITIES
  • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
  • A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
  • A61P9/00—Drugs for disorders of the cardiovascular system
  • A61P9/12—Antihypertensives

Definitions

• Embodiments of the present invention are related to using compositions of cicletanine and PKC inhibitors, either alone, or in combination with other agents, for the treatment of diseases such as pulmonary hypertension, chronic obstructive pulmonary disease (COPD), cor pulmonale, asthma, idiopathic pulmonary fibrosis, other pulmonary diseases and associated complications of these diseases.
• diseases such as pulmonary hypertension, chronic obstructive pulmonary disease (COPD), cor pulmonale, asthma, idiopathic pulmonary fibrosis, other pulmonary diseases and associated complications of these diseases.
• COPD chronic obstructive pulmonary disease
• Pulmonary hypertension is a relatively rare disease in which, generally speaking, the pulmonary vasculature undergoes pathologic changes resulting in elevated pulmonary artery pressures with concomitant increase in right ventricular workload. The illness is typically progressive and fatal. Untreated survival is approximately 3 years. Treatment options are relatively limited
• the cause of PH is not known and is likely multifactoral, rendering accurate prediction of efficacy for possible treatment approaches prior to clinical trials very difficult.
• the disease entity has been characterized by the World Health Organization (WHO) into several classes based upon pathologic states that may have some relevance to the underlying causes of the disease. It is generally thought that different treatment modalities may be required for the different classes, and indeed, some differences in response to treatment have been noted even within different sub categories of each individual class. So far, agents approved for treatment of WHO I category have not yet been approved for the other categories, and there have been several failed clinical trials for such agents in WHO category Ill. Even the approved drugs are often limited in application to certain functional levels within the class, based upon risk and benefit assessment. WHO category I is thought to have a prevalence of around 40,000 patients.
• Pulmonary fibrosis is an even rarer condition than pulmonary hypertension. It can be caused by a variety of insults to the pulmonary parenchymal tissue, but most commonly there is no clear clause, hence it is referred to as idiopathic. This form of the disease has a US prevalence of around 10,000. It's pathophysiology is unclear, but results in loss of elastic tissue in the lung, resulting in restricted lung capacity and inadequate oxygenation. There are no fully satisfactory treatments, but some forms respond to immune suppression.
• Chronic Obstructive Pulmonary Disease also involves the loss of alveolar tissue as well. They are a major cause of morbidity and mortality. Current treatments are largely palliative and do not slow the underlying disease progression. Current US prevalence is 19,000,000.
• therapeutically beneficial formulations comprising a therapeutically effective amount of cicletanine alone, or in combination with one or more second agents, or of ruboxistaurin alone, or in combination with cicletanine and/or other agents for the treatment of pulmonary hypertension and other pulmonary diseases, as well as the complications arising from such diseases.
• High dosage racemic cicletanine has been used somewhat successfully in clinical trials and in the practice of medicine as a hypertension agent. However, it has never been approved for treatment of disease other than as a thiazide like diuretic for treatment of essential hypertension in a few European countries. Its mechanism of action is poorly understood, but it is known in some instances to have diuretic effects and also to act as a vasodilator in isolated tissue models at very high doses, doses that are likely impossible to practically achieve in living organisms.
• Cicletanine is an effective agent for the treatment of pulmonary hypertension, despite the fact that it may act as a vasodilator, a class of drugs that has not been found to be generally effective for producing long term clinical improvement of pulmonary hypertension.
• the inventors also have identified means for further improving cicletanine effectiveness, and for targeting such improvements to specific classes of pulmonary hypertension.
• the inventors have unexpectedly discovered that Cicletanine will be effective for treatment of PH in all of the current WHO classes, based among other reasons upon its beneficial effects on endothelial function, which results in reduced tissue hyperproliferation and in improved coagulation parameters.
• cicletanine yields favorable, long-term hemodynamic and clinical improvements from baseline in pulmonary hypertension associated with left-sided heart failure.
• Cicletanine demonstrates clinical benefit in WHO class II patients as well. When dosed orally once daily at 50 mg daily, improvements in functional status as measured by improved 12 minute walking distance were observed.
• Cicletanine is effective in treatment of complications of pulmonary hypertension, such as heart failure.
• Heart failure usually right-sided heart failure
• WHO class III heart failure
• Natriuretic peptide level a marker of heart failure is improved by oral administration of 150 mg of Cicletanine daily to a human subject with heart failure.
• Cicletanine in some patient populations at doses up to 400 mg. Consequently the favorable effects of cicletanine in heart failure can be achieved safely by increasing the dosage significantly above that used in current practice. This is particularly effective by use of means to reduce or modulate the magnitude of the kaliuretic, natriuretic and diuretic effects of Cicletanine. As part of aspects of the present invention, and as described below, we have also invented several means of accomplishing this objective.
• a number of chemical compounds produce elevations in vascular nitric oxide levels. Such elevation can be helpful in treatment of disease, but can also worsen some disease states. Many compounds that elevate nitric oxide quickly lose efficacy over a matter of a few hours or days (tachyphylaxis) and require episodic dosing. During the off period of such dosing the disease process may continue or worsen.
• tachyphylaxis achyphylaxis
• cicletanine increases nitric oxide in deficiency states without producing excessive levels that actually cause tissue damage. It also avoids or prevents tachyphylaxis.
• a compound, which we call a nitric oxide modulating agent is effective in treating numerous cardiac and pulmonary disorders, by improving the function of vascular endothelium.
• furopyridine compounds and cicletanine in particular have the desired nitric oxide modulating properties.
• Cicletanine produces increased levels of nitric oxide in vascular tissue and that this effect is persistent across a wide range of concentrations, corresponding to human doses ranging from 1 mg daily to several thousand milligrams daily. We have found that it does so by enhancing endogenous nitric oxide production and it also avoids tachyphylaxis to its own effects and prevents tachyphylaxis to other nitrogen enhancing drugs.
• Ruboxistaurin is a protein kinase C beta isoform inhibitor. It has undergone extensive investigation for treatment of diabetes complications with equivocal results. The FDA has recently notified its sponsor that a large additional successful clinical trial will be required before the drug can be approved in the US for treatment of Diabetic complications.
• ruboxistaurin makes it suitable agent for treatment of pulmonary hypertension, alone or in combination with Cicletanine. In particular it modulates the adverse effects of vascular endothelial dysfunction and dysregulated nitric oxide production.
• inhibition of the beta isoform of protein kinase C will have favorable effects upon nitric oxide levels.
• nitric oxide modulating agents as follows:
• PKC-beta inhibitors and more in particular ruboxistaurin and cicletanine (either alone or in combination with each other) in the treatment of pulmonary and cardiac disease.
• Cerletanine when used herein when unmodified by such descriptors as racemic, enantiomeric, non-racemic, is intended to include any and all of these chemical entities: racemic cicletanine, ( ⁇ ) cicletanine enantiomer, (+) cicletanine enantiomer, non-racemic mixtures of the two cicletanine enantiomers.
• a successful clinical trial of one of the embodiments comprised use of racemic cicletanine with the dosage initiated at 50 mg daily and titrated as tolerated to 150 mg daily in a patient with Class I Pulmonary Hypertension.
• This treatment has resulted in substantial improvement in functional status as measured by a more than 12 fold increase in walking distance and substantial reductions in natriuretic peptide serum levels, demonstrating improved cardiac function.
• Another embodiment comprises the use of 50 mg oral daily doses of racemic cicletanine for treatment of Class II Pulmonary Hypertension, resulting in improved walking distance values.
• Yet another embodiment comprises the use of 50 mg oral daily doses of racemic cicletanine for treatment of Class III Pulmonary Hypertension, resulting in improved NYHA functional status.
• the certain embodiments of the invention will include a wide range of doses, titrated to main effects and side effects. Differences in absorption, distribution, and excretion may further increase the dose range.
• certain embodiments of the invention include doses as low as 1 mg, and as high as 10,000 milligrams of cicletanine.
• Use of drug blood levels, biomarker levels, and clinical response allow particularization of individual doses to maximize effect and minimize adverse side effects.
• the various cicletanine and/or ruboxistaurin compositions may be the only active ingredients of the formulation.
• a second, third, or fourth agent may be combined along with the cicletanine and/or ruboxistaurin.
• Agent refers to any pharmaceutically active agent other than cicletanine or ruboxistaurin. Such agents may be by themselves effective agents for treatment of pulmonary disease, or may enhance the effectiveness of cicletanine, ruboxistaurin or other agents contained in the combination therapy.
• Such agents may include prostacyclins and their analogues, xprostacyclin inducers, endothelin antagonists, phosphodiesterase inhibitors, anti-histamines, calcium channel blockers, cGMP activators, nitrogen or nitric oxide enhancers or donors for treatment of pulmonary hypertension.
• agents may include beta blockers, digitalis derivatives, phosphodiesterase inhibitors, vasodilators, and diuretics.
• immune modulators such as steroids, leukotriene inhibitors, beta agonists, and mast cell inhibitors such as cromolyn.
• the range of diseases and associated complications or sequalae that receive benefit from cicletanine or ruboxistaurin alone are understood to derive further benefit from the combination formulations.
• an oral therapeutic formulation wherein sufficient cicletanine is contained to improve pulmonary hemodynamics without excessive lowering of systemic blood pressure.
• Excessive reduction of systemic blood pressure has been a limiting side effect in many agents potentially useful for treatment of pulmonary hypertension.
• Our data shows that doses up to 150 mg have minimal effects on systemic blood pressure in normotensive patients.
• Use of appropriate delivery or other mechanisms to optimize blood levels of individual isomers will allow even higher dosing without adverse impacts on systemic blood pressures.
• Another embodiment may include the treatment of patients having pulmonary hypertension and other pulmonary or cardiac diseases with, either singly or in combination:
• Another of the embodiments specifically involves the use of ruboxistaurin and/or cicletanine in the treatment of WHO group I patients, [including a strategy wherein ( ⁇ ) cicletanine isomer is emphasized (e.g., in a non-racemic mixture of the two isomers that favors the ( ⁇ ) isomer) or used in its pure form], in the treatment of patients with pulmonary hypertension of WHO Group I.
• An embodiment in treatment of class I pulmonary hypertension may include initiation of therapy at 50 mg oral daily dosing with titration upward as tolerated. This embodiment may be enhanced by use of serum drug and biomarker measurements to adjust dosing.
• Another of the embodiments specifically involves the use of ruboxistaurin and/or cicletanine [including a strategy wherein ( ⁇ )cicletanine isomer is emphasized (e.g., in a non-racemic mixture of the two isomers that favors the ( ⁇ ) isomer) or used in its pure form] in the treatment of patients with pulmonary hypertension of WHO Group II.
• An embodiment in treatment of class II pulmonary hypertension may comprise initiation of therapy at 50 mg oral daily dosing with titration upward as tolerated. This embodiment may be enhanced by use of serum drug and biomarker measurements to adjust dosing.
• Another of the embodiments may comprise the use of ruboxistaurin and/or cicletanine [including a strategy wherein the ( ⁇ )cicletanine isomer is emphasized (e.g., in a non-racemic mixture of the two isomers that favors the ( ⁇ ) isomer) or used in its pure form] in the treatment of patients with pulmonary hypertension of WHO Group III.
• ( ⁇ )cicletanine as a nitric oxide enhancing agent
• the endothelial dysfunction i.e., aberrant nitric oxide regulation
• driving the pathology of this type of pulmonary hypertension e.g., PH associated with left-sided heart failure
• emphasizing the ( ⁇ ) enantiomer or using it in its pure form will yield further clinical benefits.
• An embodiment in treatment of class III pulmonary hypertension may comprise initiation of therapy at 50 mg oral daily dosing with titration upward as tolerated. This embodiment may be enhanced by use of serum drug and biomarker measurements to adjust dosing.
• Another embodiment may comprise the use of ruboxistaurin and/or cicletanine [including a strategy wherein the ( ⁇ )cicletanine isomer is emphasized (e.g., in a non-racemic mixture of the two isomers that favors the ( ⁇ ) isomer) or used in its pure form] in the treatment of patients with pulmonary hypertension of WHO Group IV.
• ruboxistaurin and/or cicletanine including a strategy wherein the ( ⁇ )cicletanine isomer is emphasized (e.g., in a non-racemic mixture of the two isomers that favors the ( ⁇ ) isomer) or used in its pure form
• the ability to address the endothelial dysfunction underlying some of the pathology of this disease with an agent distinctively able to address nitric oxide levels provides meaningful clinical benefits to patients with this disease.
• An embodiment in treatment of class IV pulmonary hypertension may comprise initiation of therapy at 50 mg oral daily dosing with titration upward as tolerated. This embodiment may be enhanced by use of serum drug and biomarker measurements to adjust dosing.
• Another embodiment may comprise the use of ruboxistaurin and/or cicletanine [including a strategy wherein the ( ⁇ )cicletanine isomer is emphasized (e.g., in a non-racemic mixture of the two isomers that favors the ( ⁇ ) isomer) or used in its pure form] in the treatment of patients with pulmonary hypertension of WHO Group V.
• ruboxistaurin and/or cicletanine including a strategy wherein the ( ⁇ )cicletanine isomer is emphasized (e.g., in a non-racemic mixture of the two isomers that favors the ( ⁇ ) isomer) or used in its pure form
• An embodiment in treatment of class IV pulmonary hypertension may comprise initiation of therapy at 50 mg oral daily dosing with titration upward as tolerated. This embodiment may be enhanced by use of serum drug and biomarker measurements to adjust dosing.
• Cicletanine in order to reduce first pass hepatic metabolism, which produces a Cicletanine metabolite that is responsible for diuretic activity, and converts the free Cicletanine responsible for its other therapeutic effects, into a metabolite that is clinically inactive.
• a time release formulation enhances Cicletanine effectiveness in cardiac disease and pulmonary hypertension, even though Cicletanine's biological activity is long lasting.
• An extended release formulation reduces peak drug levels associated with natriuresis, kaliuresis, and diuresis, while still achieving adequate levels for its endothelial protective activities. In some instances there are differences in the clearance rate between the active and inactive forms of Cicletanine that will make this strategy even more useful.
• use of agents acting in the liver to inhibit or enhance certain metabolic pathways allow for a more effective ratio of active and less active forms of Cicletanine.
• certain members of the fibrate class of drugs act to inhibit glucoronidation, which converts Cicletanine into an inactive metabolite.
• Other metabolic enhancers/inhibitors may also be used.
• a formulation incorporating 600 mg of gemfibrozil and a therapeutic amount of cicletanine as elsewhere discussed are administered once daily by mouth. Titration with initial amounts of cicletanine beginning at 10 mg and increasing to as much as 10,000 mg. are performed using clinical effect, serum levels of active drug or other biomarkers.
• nitrate, nitrite, amine, and amide salts and esters or other chemically bound nitrogen containing combinations with Cicletanine and its enantiomers to further enhance the beneficial effects of Cicletanine on the endothelium by providing further enhancement in nitric oxide levels.
• a combination formulation of cicletanine or its enantiomers or combinations of its enantiomers and a second agent that provides additional nitrogen availability such as nitroglycerin, isosorbide dinitrate, arginine or arginine containing compounds.
• Another enhancement of some embodiments is the use of cofactors and or substrates for nitric oxide production in combination with Cicletanine.
• Another embodiment may comprise use of a therapeutic amount of cicletanine formulated with a therapeutic amount of tetrahydrobiopterin (BH4) and or Arginine.
• the dose of cicletanine is titrated as heretofore discussed.
• Arginine dose is titrated from 200 mg to 1000 mg daily.
• BH4 or an orally administered analogue thereof is incorporated in a therapeutically active amount.
• Another enhancement may comprise use of nitrogen providing chemical entities that are chemically bound to the cicletanine molecule to enhance its effectiveness in modulating endothelial function.
• the embodiments disclosed herein may comprise and/or be applied to racemic, non-racemic and pure enantiomeric forms of Cicletanine.
• pure(+) cicletanine has beneficial effects across a narrower dose range than that of ( ⁇ ) cicletanine and racemic cicletanine, wherein enhanced prostacyclin synthesis is mediated.
• This effect can be maximized in some embodiments by dose adjustment to achieve active drug levels in the range of 10-9 to 10-7 moles/liter.
• Use of prostacyclin/thromboxane ratios and prostacyclin metabolite assays, as well as serum drug levels allows targeting for maximum benefit with minimum adverse side effects.
• (+) cicletanine is upward titration of once daily oral dosing beginning at 10 mg and titrating upward to 200 mg. This embodiment in some instances is particularly appropriate for patients in whom the diuretic and natriuretic effects of (+) cicletanine are well tolerated or helpful.
• Another embodiment of the invention is use of cicletanine alone or in combination with other agents for the treatment of asthma and COPD via cicletanine's antihistaminergic and notric oxide enhancing properties.
• cicletanine is used to reduce the side effects of other medications, such as injection site inflammation from prostacyclins or peripheral edema from calcium channel blockers.
• cicletanine is used to enhance the effect of other therapeutic agents, thereby allowing lower dosing with an enhanced side effect profile.
• cicletanine is used in combination with another agent or agents to allow a combined medication dosage to be more effective than that of similar doses of the individual agents, thereby reducing side effect frequency or severity.
• the combination therapies comprise fixed does (of each component), in single tablet or capsule form, or other appropriate oral formulation with appropriate excipients, dissolution enhancers and stabilizers.
• combination therapy simplifies treatment regimens, and supports patient compliance. Provision of multiple combination does still allows for variation in total doses for appropriate tailoring of therapy
• compositions below involve total dosages of 150 mg
• therapeutic dosages in related Examples may range from 1 mg to 10000 mg.
• the medications described may include modifications to enhance effect as discussed above, as well as combinations with one or more of any members of the classes of drugs including prostacyclin analogues such as eprostenol, iloprost, and treprostinil, endothelin antagonists, such as bosentan, PDE inhibitors, such as sildenafil, calcium channel blockers, such as nifedipine, amlodipine, and nicardipine, nitrogen donors, such as sodium nitroprusside, and cGMP inducers or enhancers, such as atrial natriuretic peptide, and serotonin inhibitors.
• prostacyclin analogues such as eprostenol, iloprost, and treprostinil
• endothelin antagonists such as bosentan
• PDE inhibitors such as sildenafil
• Cicletanine therapy was inititiated—oral once daily, titrating from 50 mg to 150 mg/day over three days—day 1 at 50 mg, day 2 at 100 mg, day 3 and thereafter at 150 mg.
• the patient has manifested a significant improvement in 6-minute walking distance, which was less than 30 meters immediately prior to cicletanine initiation, and was over 200 meters after one month of cicletanine therapy and was over 400 meters from the second month of cicletanine therapy onward.
• N-terminal pro-B-type natriuretic peptide an accepted biomarker of cardiac failure
• a cicletanine formulation comprising 200 mg of (+) cicletanine is administered via an oral route once daily, to patients with WHO group I pulmonary hypertension.
• Cicletanine is administered alone or in combination with other classes of drugs as discussed above.
• pulmonary hemodynamics are improved, systemic blood pressure remains within acceptable limits, and in addition one or more of the following parameters is improved: BNP levels, walking distance, prostacyclin/thromboxane ratio, and NYHA functional class score. Metabolic parameters remain unchanged or improved. Such improvements remain above baseline for at least 3 months.
• Such a formulation has a prominent diuretic effect and is most appropriate for patients experiencing substantial fluid overload.
• a cicletanine formulation comprising 180 mg of (+) cicletanine and 20 mg of ( ⁇ ) cicletanine is administered via an oral route once daily, to patients with WHO group I pulmonary hypertension.
• Cicletanine is administered alone or in combination with other classes of drugs as discussed above.
• pulmonary hemodynamics are improved, systemic blood pressure remains within acceptable limits, and in addition one or more of the following parameters is improved: BNP levels, walking distance, prostacyclin/thromboxane ratio, and NYHA functional class score. Metabolic parameters remain unchanged or improved. Such improvements remain above baseline for at least 3 months.
• Such a formulation has a prominent diuretic effect and is most appropriate for patients experiencing substantial fluid overload.
• a cicletanine formulation comprising 160 mg of (+) cicletanine and 40 mg of ( ⁇ ) cicletanine is administered via an oral route once daily, to patients with WHO group I pulmonary hypertension.
• Cicletanine is administered alone or in combination with other classes of drugs as discussed above.
• pulmonary hemodynamics are improved, systemic blood pressure remains within acceptable limits, and in addition one or more of the following parameters is improved: BNP levels, walking distance, prostacyclin/thromboxane ratio, and NYHA functional class score. Metabolic parameters remain unchanged or improved. Such improvements remain above baseline for at least 3 months.
• Such a formulation has a prominent diuretic effect and is most appropriate for patients experiencing substantial fluid overload.
• a cicletanine formulation comprising 140 mg of (+) cicletanine and 60 mg of ( ⁇ ) cicletanine is administered via an oral route once daily, to patients with WHO group I pulmonary hypertension.
• Cicletanine is administered alone or in combination with other classes of drugs as discussed above.
• pulmonary hemodynamics are improved, systemic blood pressure remains within acceptable limits, and in addition one or more of the following parameters is improved: BNP levels, walking distance, prostacyclin/thromboxane ratio, and NYHA functional class score. Metabolic parameters remain unchanged or improved. Such improvements remain above baseline for at least 3 months.
• Such a formulation has a less prominent diuretic effect and is most appropriate for patients experiencing midrange fluid overload.
• a cicletanine formulation comprising 120 mg of (+) cicletanine and 80 mg of ( ⁇ ) cicletanine is administered via an oral route once daily, to patients with WHO group I pulmonary hypertension.
• Cicletanine is administered alone or in combination with other classes of drugs as discussed above.
• pulmonary hemodynamics are improved, systemic blood pressure remains within acceptable limits, and in addition one or more of the following parameters is improved: BNP levels, walking distance, prostacyclin/thromboxane ratio, and NYHA functional class score. Metabolic parameters remain unchanged or improved. Such improvements remain above baseline for at least 3 months.
• Such a formulation has a less prominent diuretic effect and is most appropriate for patients experiencing intermediate fluid overload.
• a cicletanine formulation comprising 100 mg of (+) cicletanine and 100 mg of ( ⁇ ) cicletanine is administered via an oral route once daily, to patients with WHO group I pulmonary hypertension.
• Cicletanine is administered alone or in combination with other classes of drugs as discussed above.
• pulmonary hemodynamics are improved, systemic blood pressure remains within acceptable limits, and in addition one or more of the following parameters is improved: BNP levels, walking distance, prostacyclin/thromboxane ratio, and NYHA functional class score. Metabolic parameters remain unchanged or improved. Such improvements remain above baseline for at least 3 months.
• Such a formulation has a mid range diuretic effect and is most appropriate for patients experiencing intermediate fluid overload.
• a cicletanine formulation comprising 80 mg of (+) cicletanine and 120 mg of ( ⁇ ) cicletanine is administered via an oral route once daily, to patients with WHO group I pulmonary hypertension.
• Cicletanine is administered alone or in combination with other classes of drugs as discussed above.
• pulmonary hemodynamics are improved, systemic blood pressure remains within acceptable limits, and in addition one or more of the following parameters is improved: BNP levels, walking distance, prostacyclin/thromboxane ratio, and NYHA functional class score. Metabolic parameters remain unchanged or improved. Such improvements remain above baseline for at least 3 months.
• Such a formulation has a less prominent diuretic effect and is most appropriate for patients experiencing intermediate fluid overload.
• a cicletanine formulation comprising 60 mg of (+) cicletanine and 140 mg of ( ⁇ ) cicletanine is administered via an oral route once daily, to patients with WHO group I pulmonary hypertension.
• Cicletanine is administered alone or in combination with other classes of drugs as discussed above.
• pulmonary hemodynamics are improved, systemic blood pressure remains within acceptable limits, and in addition one or more of the following parameters is improved: BNP levels, walking distance, prostacyclin/thromboxane ratio, and NYHA functional class score. Metabolic parameters remain unchanged or improved. Such improvements remain above baseline for at least 3 months.
• Such a formulation has a less prominent diuretic effect and is most appropriate for patients experiencing intermediate fluid overload.
• a cicletanine formulation comprising 40 mg of (+) cicletanine and 160 mg of ( ⁇ ) cicletanine is administered via an oral route once daily, to patients with WHO group I pulmonary hypertension.
• Cicletanine is administered alone or in combination with other classes of drugs as discussed above.
• pulmonary hemodynamics are improved, systemic blood pressure remains within acceptable limits, and in addition one or more of the following parameters is improved: BNP levels, walking distance, prostacyclin/thromboxane ratio, and NYHA functional class score. Metabolic parameters remain unchanged or improved. Such improvements remain above baseline for at least 3 months.
• Such a formulation has a mild diuretic effect and strong nitric oxide effect and is most appropriate for patients experiencing modest fluid overload.
• a cicletanine formulation comprising 20 mg of (+) cicletanine and 180 mg of ( ⁇ ) cicletanine is administered via an oral route once daily, to patients with WHO group I pulmonary hypertension.
• Cicletanine is administered alone or in combination with other classes of drugs as discussed above.
• pulmonary hemodynamics are improved, systemic blood pressure remains within acceptable limits, and in addition one or more of the following parameters is improved: BNP levels, walking distance, prostacyclin/thromboxane ratio, and NYHA functional class score. Metabolic parameters remain unchanged or improved. Such improvements remain above baseline for at least 3 months.
• Such a formulation has a mild diuretic effect and strong nitric oxide effects and is most appropriate for patients experiencing modest fluid overload or no fluid overload.
• a cicletanine formulation comprising 200 mg of ( ⁇ ) cicletanine is administered via an oral route once daily, to patients with WHO group I pulmonary hypertension.
• Cicletanine is administered alone or in combination with other classes of drugs as discussed above.
• pulmonary hemodynamics are improved, systemic blood pressure remains within acceptable limits, and in addition one or more of the following parameters is improved: BNP levels, walking distance, prostacyclin/thromboxane ratio, and NYHA functional class score. Metabolic parameters remain unchanged or improved. Such improvements remain above baseline for at least 3 months.
• This formulation has little or no diuretic effect, and maximal nitric oxide effect and is best suited to patients with no fluid overload.
• a cicletanine formulation comprising 200 mg of (+) cicletanine is administered via an oral route once daily, to patients with WHO group II pulmonary hypertension.
• Cicletanine is administered alone or in combination with other classes of drugs as discussed above.
• pulmonary hemodynamics are improved, systemic blood pressure remains within acceptable limits, and in addition one or more of the following parameters is improved: BNP levels, walking distance, prostacyclin/thromboxane ratio, and NYHA functional class score. Metabolic parameters remain unchanged or improved. Such improvements remain above baseline for at least 3 months.
• Such a formulation has a prominent diuretic effect and is most appropriate for patients experiencing substantial fluid overload.
• a cicletanine formulation comprising 180 mg of (+) cicletanine and 20 mg of ( ⁇ ) cicletanine is administered via an oral route once daily, to patients with WHO group II pulmonary hypertension.
• Cicletanine is administered alone or in combination with other classes of drugs as discussed above.
• pulmonary hemodynamics are improved, systemic blood pressure remains within acceptable limits, and in addition one or more of the following parameters is improved: BNP levels, walking distance, prostacyclin/thromboxane ratio, and NYHA functional class score. Metabolic parameters remain unchanged or improved. Such improvements remain above baseline for at least 3 months.
• Such a formulation has a mild diuretic effect and strong nitric oxide effects and is most appropriate for patients experiencing modest fluid overload or no fluid overload.
• a cicletanine formulation comprising 160 mg of (+) cicletanine and 40 mg of ( ⁇ ) cicletanine is administered via an oral route once daily, to patients with WHO group II pulmonary hypertension.
• Cicletanine is administered alone or in combination with other classes of drugs as discussed above.
• pulmonary hemodynamics are improved, systemic blood pressure remains within acceptable limits, and in addition one or more of the following parameters is improved: BNP levels, walking distance, prostacyclin/thromboxane ratio, and NYHA functional class score. Metabolic parameters remain unchanged or improved. Such improvements remain above baseline for at least 3 months.
• Such a formulation has a prominent diuretic effect and is most appropriate for patients experiencing substantial fluid overload.
• a cicletanine formulation comprising 140 mg of (+) cicletanine and 60 mg of ( ⁇ ) cicletanine is administered via an oral route once daily, to patients with WHO group II pulmonary hypertension.
• Cicletanine is administered alone or in combination with other classes of drugs as discussed above.
• pulmonary hemodynamics are improved, systemic blood pressure remains within acceptable limits, and in addition one or more of the following parameters is improved: BNP levels, walking distance, prostacyclin/thromboxane ratio, and NYHA functional class score. Metabolic parameters remain unchanged or improved. Such improvements remain above baseline for at least 3 months.
• Such a formulation has a less prominent diuretic effect and is most appropriate for patients experiencing midrange fluid overload.
• a cicletanine formulation comprising 120 mg of (+) cicletanine and 80 mg of ( ⁇ ) cicletanine is administered via an oral route once daily, to patients with WHO group II pulmonary hypertension.
• Cicletanine is administered alone or in combination with other classes of drugs as discussed above.
• pulmonary hemodynamics are improved, systemic blood pressure remains within acceptable limits, and in addition one or more of the following parameters is improved: BNP levels, walking distance, prostacyclin/thromboxane ratio, and NYHA functional class score. Metabolic parameters remain unchanged or improved. Such improvements remain above baseline for at least 3 months.
• Such a formulation has a less prominent diuretic effect and is most appropriate for patients experiencing intermediate fluid overload.
• a cicletanine formulation comprising 100 mg of (+) cicletanine and 100 mg of ( ⁇ ) cicletanine is administered via an oral route once daily, to patients with WHO group II pulmonary hypertension.
• Cicletanine is administered alone or in combination with other classes of drugs as discussed above.
• pulmonary hemodynamics are improved, systemic blood pressure remains within acceptable limits, and in addition one or more of the following parameters is improved: BNP levels, walking distance, prostacyclin/thromboxane ratio, and NYHA functional class score. Metabolic parameters remain unchanged or improved. Such improvements remain above baseline for at least 3 months.
• Such a formulation has a mid range diuretic effect and is most appropriate for patients experiencing intermediate fluid overload.
• a cicletanine formulation comprising 80 mg of (+) cicletanine and 120 mg of ( ⁇ ) cicletanine is administered via an oral route once daily, to patients with WHO group II pulmonary hypertension.
• Cicletanine is administered alone or in combination with other classes of drugs as discussed above.
• pulmonary hemodynamics are improved, systemic blood pressure remains within acceptable limits, and in addition one or more of the following parameters is improved: BNP levels, walking distance, prostacyclin/thromboxane ratio, and NYHA functional class score. Metabolic parameters remain unchanged or improved. Such improvements remain above baseline for at least 3 months.
• Such a formulation has a less prominent diuretic effect and is most appropriate for patients experiencing intermediate fluid overload.
• a cicletanine formulation comprising 60 mg of (+) cicletanine and 140 mg of ( ⁇ ) cicletanine is administered via an oral route once daily, to patients with WHO group II pulmonary hypertension.
• Cicletanine is administered alone or in combination with other classes of drugs as discussed above.
• pulmonary hemodynamics are improved, systemic blood pressure remains within acceptable limits, and in addition one or more of the following parameters is improved: BNP levels, walking distance, prostacyclin/thromboxane ratio, and NYHA functional class score. Metabolic parameters remain unchanged or improved. Such improvements remain above baseline for at least 3 months.
• Such a formulation has a less prominent diuretic effect and is most appropriate for patients experiencing intermediate fluid overload.
• a cicletanine formulation comprising 40 mg of (+) cicletanine and 160 mg of ( ⁇ ) cicletanine is administered via an oral route once daily, to patients with WHO group II pulmonary hypertension.
• Cicletanine is administered alone or in combination with other classes of drugs as discussed above.
• pulmonary hemodynamics are improved, systemic blood pressure remains within acceptable limits, and in addition one or more of the following parameters is improved: BNP levels, walking distance, prostacyclin/thromboxane ratio, and NYHA functional class score. Metabolic parameters remain unchanged or improved. Such improvements remain above baseline for at least 3 months.
• Such a formulation has a mild diuretic effect and strong nitric oxide effect and is most appropriate for patients experiencing modest fluid overload.
• a cicletanine formulation comprising 20 mg of (+) cicletanine and 180 mg of ( ⁇ ) cicletanine is administered via an oral route once daily, to patients with WHO group II pulmonary hypertension.
• Cicletanine is administered alone or in combination with other classes of drugs as discussed above.
• pulmonary hemodynamics are improved, systemic blood pressure remains within acceptable limits, and in addition one or more of the following parameters is improved: BNP levels, walking distance, prostacyclin/thromboxane ratio, and NYHA functional class score. Metabolic parameters remain unchanged or improved. Such improvements remain above baseline for at least 3 months.
• Such a formulation has a mild diuretic effect and strong nitric oxide effects and is most appropriate for patients experiencing modest fluid overload or no fluid overload.
• a cicletanine formulation comprising 200 mg of ( ⁇ ) cicletanine is administered via an oral route once daily, to patients with WHO group II pulmonary hypertension.
• Cicletanine is administered alone or in combination with other classes of drugs as discussed above.
• pulmonary hemodynamics are improved, systemic blood pressure remains within acceptable limits, and in addition one or more of the following parameters is improved: BNP levels, walking distance, prostacyclin/thromboxane ratio, and NYHA functional class score. Metabolic parameters remain unchanged or improved. Such improvements remain above baseline for at least 3 months.
• This formulation has little or no diuretic effect, and maximal nitric oxide effect and is best suited to patients with no fluid overload.
• a cicletanine formulation comprising 200 mg of (+) cicletanine is administered via an oral route once daily, to patients with WHO group II pulmonary hypertension.
• Cicletanine is administered alone or in combination with other classes of drugs as discussed above.
• pulmonary hemodynamics are improved, systemic blood pressure remains within acceptable limits, and in addition one or more of the following parameters is improved: BNP levels, walking distance, prostacyclin/thromboxane ratio, and NYHA functional class score. Metabolic parameters remain unchanged or improved. Such improvements remain above baseline for at least 3 months.
• Such a formulation has a mild diuretic effect and strong nitric oxide effects and is most appropriate for patients experiencing modest fluid overload or no fluid overload.
• a cicletanine formulation comprising 180 mg of (+) cicletanine and 20 mg of ( ⁇ ) cicletanine is administered via an oral route once daily, to patients with WHO group III pulmonary hypertension.
• Cicletanine is administered alone or in combination with other classes of drugs as discussed above.
• pulmonary hemodynamics are improved, systemic blood pressure remains within acceptable limits, and in addition one or more of the following parameters is improved: BNP levels, walking distance, prostacyclin/thromboxane ratio, and NYHA functional class score. Metabolic parameters remain unchanged or improved. Such improvements remain above baseline for at least 3 months.
• Such a formulation has a prominent diuretic effect and is most appropriate for patients experiencing substantial fluid overload.
• a cicletanine formulation comprising 160 mg of (+) cicletanine and 40 mg of ( ⁇ ) cicletanine is administered via an oral route once daily, to patients with WHO group III pulmonary hypertension.
• Cicletanine is administered alone or in combination with other classes of drugs as discussed above.
• pulmonary hemodynamics are improved, systemic blood pressure remains within acceptable limits, and in addition one or more of the following parameters is improved: BNP levels, walking distance, prostacyclin/thromboxane ratio, and NYHA functional class score. Metabolic parameters remain unchanged or improved. Such improvements remain above baseline for at least 3 months.
• Such a formulation has a prominent diuretic effect and is most appropriate for patients experiencing substantial fluid overload.
• a cicletanine formulation comprising 140 mg of (+) cicletanine and 60 mg of ( ⁇ ) cicletanine is administered via an oral route once daily, to patients with WHO group III pulmonary hypertension.
• Cicletanine is administered alone or in combination with other classes of drugs as discussed above.
• pulmonary hemodynamics are improved, systemic blood pressure remains within acceptable limits, and in addition one or more of the following parameters is improved: BNP levels, walking distance, prostacyclin/thromboxane ratio, and NYHA functional class score. Metabolic parameters remain unchanged or improved. Such improvements remain above baseline for at least 3 months.
• Such a formulation has a less prominent diuretic effect and is most appropriate for patients experiencing midrange fluid overload.
• a cicletanine formulation comprising 120 mg of (+) cicletanine and 80 mg of ( ⁇ ) cicletanine is administered via an oral route once daily, to patients with WHO group III pulmonary hypertension.
• Cicletanine is administered alone or in combination with other classes of drugs as discussed above.
• pulmonary hemodynamics are improved, systemic blood pressure remains within acceptable limits, and in addition one or more of the following parameters is improved: BNP levels, walking distance, prostacyclin/thromboxane ratio, and NYHA functional class score. Metabolic parameters remain unchanged or improved. Such improvements remain above baseline for at least 3 months.
• Such a formulation has a less prominent diuretic effect and is most appropriate for patients experiencing intermediate fluid overload.
• a cicletanine formulation comprising 100 mg of (+) cicletanine and 100 mg of ( ⁇ ) cicletanine is administered via an oral route once daily, to patients with WHO group III pulmonary hypertension.
• Cicletanine is administered alone or in combination with other classes of drugs as discussed above.
• pulmonary hemodynamics are improved, systemic blood pressure remains within acceptable limits, and in addition one or more of the following parameters is improved: BNP levels, walking distance, prostacyclin/thromboxane ratio, and NYHA functional class score. Metabolic parameters remain unchanged or improved. Such improvements remain above baseline for at least 3 months.
• Such a formulation has a mid range diuretic effect and is most appropriate for patients experiencing intermediate fluid overload.
• a cicletanine formulation comprising 80 mg of (+) cicletanine and 120 mg of ( ⁇ ) cicletanine is administered via an oral route once daily, to patients with WHO group III pulmonary hypertension.
• Cicletanine is administered alone or in combination with other classes of drugs as discussed above.
• pulmonary hemodynamics are improved, systemic blood pressure remains within acceptable limits, and in addition one or more of the following parameters is improved: BNP levels, walking distance, prostacyclin/thromboxane ratio, and NYHA functional class score. Metabolic parameters remain unchanged or improved. Such improvements remain above baseline for at least 3 months.
• Such a formulation has a less prominent diuretic effect and is most appropriate for patients experiencing intermediate fluid overload.
• a cicletanine formulation comprising 60 mg of (+) cicletanine and 140 mg of ( ⁇ ) cicletanine is administered via an oral route once daily, to patients with WHO group III pulmonary hypertension.
• Cicletanine is administered alone or in combination with other classes of drugs as discussed above.
• pulmonary hemodynamics are improved, systemic blood pressure remains within acceptable limits, and in addition one or more of the following parameters is improved: BNP levels, walking distance, prostacyclin/thromboxane ratio, and NYHA functional class score. Metabolic parameters remain unchanged or improved. Such improvements remain above baseline for at least 3 months.
• Such a formulation has a less prominent diuretic effect and is most appropriate for patients experiencing intermediate fluid overload.
• a cicletanine formulation comprising 40 mg of (+) cicletanine and 160 mg of ( ⁇ ) cicletanine is administered via an oral route once daily, to patients with WHO group III pulmonary hypertension.
• Cicletanine is administered alone or in combination with other classes of drugs as discussed above.
• pulmonary hemodynamics are improved, systemic blood pressure remains within acceptable limits, and in addition one or more of the following parameters is improved: BNP levels, walking distance, prostacyclin/thromboxane ratio, and NYHA functional class score. Metabolic parameters remain unchanged or improved. Such improvements remain above baseline for at least 3 months.
• Such a formulation has a mild diuretic effect and strong nitric oxide effect and is most appropriate for patients experiencing modest fluid overload.
• a cicletanine formulation comprising 20 mg of (+) cicletanine and 180 mg of ( ⁇ ) cicletanine is administered via an oral route once daily, to patients with WHO group III pulmonary hypertension.
• Cicletanine is administered alone or in combination with other classes of drugs as discussed above.
• pulmonary hemodynamics are improved, systemic blood pressure remains within acceptable limits, and in addition one or more of the following parameters is improved: BNP levels, walking distance, prostacyclin/thromboxane ratio, and NYHA functional class score. Metabolic parameters remain unchanged or improved. Such improvements remain above baseline for at least 3 months.
• Such a formulation has a mild diuretic effect and strong nitric oxide effects and is most appropriate for patients experiencing modest fluid overload or no fluid overload.
• a cicletanine formulation comprising 200 mg of ( ⁇ ) cicletanine is administered via an oral route once daily, to patients with WHO group III pulmonary hypertension.
• Cicletanine is administered alone or in combination with other classes of drugs as discussed above.
• pulmonary hemodynamics are improved, systemic blood pressure remains within acceptable limits, and in addition one or more of the following parameters is improved: BNP levels, walking distance, prostacyclin/thromboxane ratio, and NYHA functional class score. Metabolic parameters remain unchanged or improved. Such improvements remain above baseline for at least 3 months.
• Such a formulation has a mild diuretic effect and strong nitric oxide effects and is most appropriate for patients experiencing modest fluid overload or no fluid overload.
• a cicletanine formulation comprising 200 mg of (+) cicletanine is administered via an oral route once daily, to patients with WHO group IV pulmonary hypertension.
• Cicletanine is administered alone or in combination with other classes of drugs as discussed above.
• pulmonary hemodynamics are improved, systemic blood pressure remains within acceptable limits, and in addition one or more of the following parameters is improved: BNP levels, walking distance, prostacyclin/thromboxane ratio, and NYHA functional class score. Metabolic parameters remain unchanged or improved. Such improvements remain above baseline for at least 3 months.
• Such a formulation has a prominent diuretic effect and is most appropriate for patients experiencing substantial fluid overload.
• a cicletanine formulation comprising 180 mg of (+) cicletanine and 20 mg of ( ⁇ ) cicletanine is administered via an oral route once daily, to patients with WHO group IV pulmonary hypertension.
• Cicletanine is administered alone or in combination with other classes of drugs as discussed above.
• pulmonary hemodynamics are improved, systemic blood pressure remains within acceptable limits, and in addition one or more of the following parameters is improved: BNP levels, walking distance, prostacyclin/thromboxane ratio, and NYHA functional class score. Metabolic parameters remain unchanged or improved. Such improvements remain above baseline for at least 3 months.
• Such a formulation has a prominent diuretic effect and is most appropriate for patients experiencing substantial fluid overload.
• a cicletanine formulation comprising 160 mg of (+) cicletanine and 40 mg of ( ⁇ ) cicletanine is administered via an oral route once daily, to patients with WHO group IV pulmonary hypertension.
• Cicletanine is administered alone or in combination with other classes of drugs as discussed above.
• pulmonary hemodynamics are improved, systemic blood pressure remains within acceptable limits, and in addition one or more of the following parameters is improved: BNP levels, walking distance, prostacyclin/thromboxane ratio, and NYHA functional class score. Metabolic parameters remain unchanged or improved. Such improvements remain above baseline for at least 3 months.
• Such a formulation has a prominent diuretic effect and is most appropriate for patients experiencing substantial fluid overload.
• a cicletanine formulation comprising 140 mg of (+) cicletanine and 60 mg of ( ⁇ ) cicletanine is administered via an oral route once daily, to patients with WHO group IV pulmonary hypertension.
• Cicletanine is administered alone or in combination with other classes of drugs as discussed above.
• pulmonary hemodynamics are improved, systemic blood pressure remains within acceptable limits, and in addition one or more of the following parameters is improved: BNP levels, walking distance, prostacyclin/thromboxane ratio, and NYHA functional class score. Metabolic parameters remain unchanged or improved. Such improvements remain above baseline for at least 3 months.
• Such a formulation has a less prominent diuretic effect and is most appropriate for patients experiencing midrange fluid overload.
• a cicletanine formulation comprising 120 mg of (+) cicletanine and 80 mg of ( ⁇ ) cicletanine is administered via an oral route once daily, to patients with WHO group IV pulmonary hypertension.
• Cicletanine is administered alone or in combination with other classes of drugs as discussed above.
• pulmonary hemodynamics are improved, systemic blood pressure remains within acceptable limits, and in addition one or more of the following parameters is improved: BNP levels, walking distance, prostacyclin/thromboxane ratio, and NYHA functional class score. Metabolic parameters remain unchanged or improved. Such improvements remain above baseline for at least 3 months.
• Such a formulation has a less prominent diuretic effect and is most appropriate for patients experiencing intermediate fluid overload.
• a cicletanine formulation comprising 100 mg of (+) cicletanine and 100 mg of ( ⁇ ) cicletanine is administered via an oral route once daily, to patients with WHO group IV pulmonary hypertension.
• Cicletanine is administered alone or in combination with other classes of drugs as discussed above.
• pulmonary hemodynamics are improved, systemic blood pressure remains within acceptable limits, and in addition one or more of the following parameters is improved: BNP levels, walking distance, prostacyclin/thromboxane ratio, and NYHA functional class score. Metabolic parameters remain unchanged or improved. Such improvements remain above baseline for at least 3 months.
• Such a formulation has a mid range diuretic effect and is most appropriate for patients experiencing intermediate fluid overload.
• a cicletanine formulation comprising 80 mg of (+) cicletanine and 120 mg of ( ⁇ ) cicletanine is administered via an oral route once daily, to patients with WHO group IV pulmonary hypertension.
• Cicletanine is administered alone or in combination with other classes of drugs as discussed above.
• pulmonary hemodynamics are improved, systemic blood pressure remains within acceptable limits, and in addition one or more of the following parameters is improved: BNP levels, walking distance, prostacyclin/thromboxane ratio, and NYHA functional class score. Metabolic parameters remain unchanged or improved. Such improvements remain above baseline for at least 3 months.
• Such a formulation has a less prominent diuretic effect and is most appropriate for patients experiencing intermediate fluid overload.
• a cicletanine formulation comprising 60 mg of (+) cicletanine and 140 mg of ( ⁇ ) cicletanine is administered via an oral route once daily, to patients with WHO group IV pulmonary hypertension.
• Cicletanine is administered alone or in combination with other classes of drugs as discussed above.
• pulmonary hemodynamics are improved, systemic blood pressure remains within acceptable limits, and in addition one or more of the following parameters is improved: BNP levels, walking distance, prostacyclin/thromboxane ratio, and NYHA functional class score. Metabolic parameters remain unchanged or improved. Such improvements remain above baseline for at least 3 months.
• Such a formulation has a less prominent diuretic effect and is most appropriate for patients experiencing intermediate fluid overload.
• a cicletanine formulation comprising 40 mg of (+) cicletanine and 160 mg of ( ⁇ ) cicletanine is administered via an oral route once daily, to patients with WHO group IV pulmonary hypertension.
• Cicletanine is administered alone or in combination with other classes of drugs as discussed above.
• pulmonary hemodynamics are improved, systemic blood pressure remains within acceptable limits, and in addition one or more of the following parameters is improved: BNP levels, walking distance, prostacyclin/thromboxane ratio, and NYHA functional class score. Metabolic parameters remain unchanged or improved. Such improvements remain above baseline for at least 3 months.
• Such a formulation has a mild diuretic effect and strong nitric oxide effect and is most appropriate for patients experiencing modest fluid overload.
• a cicletanine formulation comprising 20 mg of (+) cicletanine and 180 mg of ( ⁇ ) cicletanine is administered via an oral route once daily, to patients with WHO group IV pulmonary hypertension.
• Cicletanine is administered alone or in combination with other classes of drugs as discussed above.
• pulmonary hemodynamics are improved, systemic blood pressure remains within acceptable limits, and in addition one or more of the following parameters is improved: BNP levels, walking distance, prostacyclin/thromboxane ratio, and NYHA functional class score. Metabolic parameters remain unchanged or improved. Such improvements remain above baseline for at least 3 months.
• Such a formulation has a mild diuretic effect and strong nitric oxide effects and is most appropriate for patients experiencing modest fluid overload or no fluid overload.
• a cicletanine formulation comprising 200 mg of ( ⁇ ) cicletanine is administered via an oral route once daily, to patients with WHO group IV pulmonary hypertension.
• Cicletanine is administered alone or in combination with other classes of drugs as discussed above.
• pulmonary hemodynamics are improved, systemic blood pressure remains within acceptable limits, and in addition one or more of the following parameters is improved: BNP levels, walking distance, prostacyclin/thromboxane ratio, and NYHA functional class score. Metabolic parameters remain unchanged or improved. Such improvements remain above baseline for at least 3 months.
• This formulation has little or no diuretic effect, and maximal nitric oxide effect and is best suited to patients with no fluid overload.
• a cicletanine formulation comprising 200 mg of (+) cicletanine is administered via an oral route once daily, to patients with WHO group V pulmonary hypertension.
• Cicletanine is administered alone or in combination with other classes of drugs as discussed above.
• pulmonary hemodynamics are improved, systemic blood pressure remains within acceptable limits, and in addition one or more of the following parameters is improved: BNP levels, walking distance, prostacyclin/thromboxane ratio, and NYHA functional class score. Metabolic parameters remain unchanged or improved. Such improvements remain above baseline for at least 3 months.
• Such a formulation has a prominent diuretic effect and is most appropriate for patients experiencing substantial fluid overload.
• a cicletanine formulation comprising 180 mg of (+) cicletanine and 20 mg of ( ⁇ ) cicletanine is administered via an oral route once daily, to patients with WHO group V pulmonary hypertension.
• Cicletanine is administered alone or in combination with other classes of drugs as discussed above.
• pulmonary hemodynamics are improved, systemic blood pressure remains within acceptable limits, and in addition one or more of the following parameters is improved: BNP levels, walking distance, prostacyclin/thromboxane ratio, and NYHA functional class score. Metabolic parameters remain unchanged or improved. Such improvements remain above baseline for at least 3 months.
• Such a formulation has a prominent diuretic effect and is most appropriate for patients experiencing substantial fluid overload.
• a cicletanine formulation comprising 160 mg of (+) cicletanine and 40 mg of ( ⁇ ) cicletanine is administered via an oral route once daily, to patients with WHO group V pulmonary hypertension.
• Cicletanine is administered alone or in combination with other classes of drugs as discussed above.
• pulmonary hemodynamics are improved, systemic blood pressure remains within acceptable limits, and in addition one or more of the following parameters is improved: BNP levels, walking distance, prostacyclin/thromboxane ratio, and NYHA functional class score. Metabolic parameters remain unchanged or improved. Such improvements remain above baseline for at least 3 months.
• Such a formulation has a prominent diuretic effect and is most appropriate for patients experiencing substantial fluid overload.
• a cicletanine formulation comprising 140 mg of (+) cicletanine and 60 mg of ( ⁇ ) cicletanine is administered via an oral route once daily, to patients with WHO group V pulmonary hypertension.
• Cicletanine is administered alone or in combination with other classes of drugs as discussed above.
• pulmonary hemodynamics are improved, systemic blood pressure remains within acceptable limits, and in addition one or more of the following parameters is improved: BNP levels, walking distance, prostacyclin/thromboxane ratio, and NYHA functional class score. Metabolic parameters remain unchanged or improved. Such improvements remain above baseline for at least 3 months.
• Such a formulation has a less prominent diuretic effect and is most appropriate for patients experiencing midrange fluid overload.
• a cicletanine formulation comprising 120 mg of (+) cicletanine and 80 mg of ( ⁇ ) cicletanine is administered via an oral route once daily, to patients with WHO group V pulmonary hypertension.
• Cicletanine is administered alone or in combination with other classes of drugs as discussed above.
• pulmonary hemodynamics are improved, systemic blood pressure remains within acceptable limits, and in addition one or more of the following parameters is improved: BNP levels, walking distance, prostacyclin/thromboxane ratio, and NYHA functional class score. Metabolic parameters remain unchanged or improved. Such improvements remain above baseline for at least 3 months.
• Such a formulation has a less prominent diuretic effect and is most appropriate for patients experiencing intermediate fluid overload.
• a cicletanine formulation comprising 100 mg of (+) cicletanine and 100 mg of ( ⁇ ) cicletanine is administered via an oral route once daily, to patients with WHO group V pulmonary hypertension.
• Cicletanine is administered alone or in combination with other classes of drugs as discussed above.
• pulmonary hemodynamics are improved, systemic blood pressure remains within acceptable limits, and in addition one or more of the following parameters is improved: BNP levels, walking distance, prostacyclin/thromboxane ratio, and NYHA functional class score. Metabolic parameters remain unchanged or improved. Such improvements remain above baseline for at least 3 months.
• Such a formulation has a mid range diuretic effect and is most appropriate for patients experiencing intermediate fluid overload.
• a cicletanine formulation comprising 80 mg of (+) cicletanine and 120 mg of ( ⁇ ) cicletanine is administered via an oral route once daily, to patients with WHO group V pulmonary hypertension.
• Cicletanine is administered alone or in combination with other classes of drugs as discussed above.
• pulmonary hemodynamics are improved, systemic blood pressure remains within acceptable limits, and in addition one or more of the following parameters is improved: BNP levels, walking distance, prostacyclin/thromboxane ratio, and NYHA functional class score. Metabolic parameters remain unchanged or improved. Such improvements remain above baseline for at least 3 months.
• Such a formulation has a less prominent diuretic effect and is most appropriate for patients experiencing intermediate fluid overload.
• a cicletanine formulation comprising 60 mg of (+) cicletanine and 140 mg of ( ⁇ ) cicletanine is administered via an oral route once daily, to patients with WHO group V pulmonary hypertension.
• Cicletanine is administered alone or in combination with other classes of drugs as discussed above.
• pulmonary hemodynamics are improved, systemic blood pressure remains within acceptable limits, and in addition one or more of the following parameters is improved: BNP levels, walking distance, prostacyclin/thromboxane ratio, and NYHA functional class score. Metabolic parameters remain unchanged or improved. Such improvements remain above baseline for at least 3 months.
• Such a formulation has a less prominent diuretic effect and is most appropriate for patients experiencing intermediate fluid overload.
• a cicletanine formulation comprising 40 mg of (+) cicletanine and 160 mg of ( ⁇ ) cicletanine is administered via an oral route once daily, to patients with WHO group V pulmonary hypertension.
• Cicletanine is administered alone or in combination with other classes of drugs as discussed above.
• pulmonary hemodynamics are improved, systemic blood pressure remains within acceptable limits, and in addition one or more of the following parameters is improved: BNP levels, walking distance, prostacyclin/thromboxane ratio, and NYHA functional class score. Metabolic parameters remain unchanged or improved. Such improvements remain above baseline for at least 3 months.
• Such a formulation has a mild diuretic effect and strong nitric oxide effect and is most appropriate for patients experiencing modest fluid overload.
• a cicletanine formulation comprising 20 mg of (+) cicletanine and 180 mg of ( ⁇ ) cicletanine is administered via an oral route once daily, to patients with WHO group V pulmonary hypertension.
• Cicletanine is administered alone or in combination with other classes of drugs as discussed above.
• pulmonary hemodynamics are improved, systemic blood pressure remains within acceptable limits, and in addition one or more of the following parameters is improved: BNP levels, walking distance, prostacyclin/thromboxane ratio, and NYHA functional class score. Metabolic parameters remain unchanged or improved. Such improvements remain above baseline for at least 3 months.
• Such a formulation has a mild diuretic effect and strong nitric oxide effects and is most appropriate for patients experiencing modest fluid overload or no fluid overload.
• a cicletanine formulation comprising 200 mg of ( ⁇ ) cicletanine is administered via an oral route once daily, to patients with WHO group V pulmonary hypertension.
• Cicletanine is administered alone or in combination with other classes of drugs as discussed above.
• pulmonary hemodynamics are improved, systemic blood pressure remains within acceptable limits, and in addition one or more of the following parameters is improved: BNP levels, walking distance, prostacyclin/thromboxane ratio, and NYHA functional class score. Metabolic parameters remain unchanged or improved. Such improvements remain above baseline for at least 3 months.
• This formulation has little or no diuretic effect, and maximal nitric oxide effect, and is best suited to patients with no fluid overload.
• a cicletanine formulation comprising 200 mg of (+) cicletanine is administered via an oral route once daily, to patients with asthma, COPD, and or pulmonary fibrosis.
• Cicletanine is administered alone or in combination with other classes of drugs as discussed above.
• pulmonary function is improved or stabilized, systemic blood pressure remains within acceptable limits, and in addition one or more of the following parameters is improved: FEV1, O2 saturation, walking distance, prostacyclin/thromboxane ratio, and NYHA functional class score. Metabolic parameters remain unchanged or improved. Such improvements remain above baseline for at least 3 months.
• Such a formulation has a prominent diuretic effect and is most appropriate for patients experiencing substantial fluid overload.
• a cicletanine formulation comprising 180 mg of (+) cicletanine and 20 mg of ( ⁇ ) cicletanine is administered via an oral route once daily, to patients with asthma or COPD or pulmonary fibrosis.
• Cicletanine is administered alone or in combination with other classes of drugs as discussed above.
• pulmonary function is improved, systemic blood pressure remains within acceptable limits, and in addition one or more of the following parameters is improved: FEV1, O2 saturation, walking distance, prostacyclin/thromboxane ratio, and NYHA functional class score. Metabolic parameters remain unchanged or improved. Such improvements remain above baseline for at least 3 months.
• Such a formulation has a prominent diuretic effect and is most appropriate for patients experiencing substantial fluid overload.
• a cicletanine formulation comprising 160 mg of (+) cicletanine and 40 mg of ( ⁇ ) cicletanine is administered via an oral route once daily, to patients with asthma or COPD or pulmonary fibrosis.
• Cicletanine is administered alone or in combination with other classes of drugs as discussed above.
• pulmonary function is improved, systemic blood pressure remains within acceptable limits, and in addition one or more of the following parameters is improved: FEV1, O2 saturation, walking distance, prostacyclin/thromboxane ratio, and NYHA functional class score. Metabolic parameters remain unchanged or improved. Such improvements remain above baseline for at least 3 months.
• Such a formulation has a prominent diuretic effect and is most appropriate for patients experiencing substantial fluid overload.
• a cicletanine formulation comprising 140 mg of (+) cicletanine and 60 mg of ( ⁇ ) cicletanine is administered via an oral route once daily, to patients with asthma or COPD or pulmonary fibrosis.
• Cicletanine is administered alone or in combination with other classes of drugs as discussed above.
• pulmonary function is improved, systemic blood pressure remains within acceptable limits, and in addition one or more of the following parameters is improved: FEV1, O2 saturation, prostacyclin/thromboxane ratio, and NYHA functional class score. Metabolic parameters remain unchanged or improved. Such improvements remain above baseline for at least 3 months.
• Such a formulation has a less prominent diuretic effect and is most appropriate for patients experiencing midrange fluid overload.
• a cicletanine formulation comprising 120 mg of (+) cicletanine and 80 mg of ( ⁇ ) cicletanine is administered via an oral route once daily, to patients with asthma or COPD or pulmonary fibrosis.
• Cicletanine is administered alone or in combination with other classes of drugs as discussed above.
• pulmonary function is improved, systemic blood pressure remains within acceptable limits, and in addition one or more of the following parameters is improved: FEV1, O2 saturation, walking distance, prostacyclin/thromboxane ratio, and NYHA functional class score. Metabolic parameters remain unchanged or improved. Such improvements remain above baseline for at least 3 months.
• Such a formulation has a less prominent diuretic effect and is most appropriate for patients experiencing intermediate fluid overload.
• a cicletanine formulation comprising 100 mg of (+) cicletanine and 100 mg of ( ⁇ ) cicletanine is administered via an oral route once daily, to patients with asthma, COPD, or pulmonary fibrosis.
• Cicletanine is administered alone or in combination with other classes of drugs as discussed above.
• pulmonary function is improved or stabilized, blood pressure remains within acceptable limits, and in addition one or more of the following parameters is improved: FEV1, O2 saturation, walking distance, prostacyclin/thromboxane ratio, and NYHA functional class score. Metabolic parameters remain unchanged or improved. Such improvements remain above baseline for at least 3 months.
• Such a formulation has a mid range diuretic effect and is most appropriate for patients experiencing intermediate fluid overload.
• a cicletanine formulation comprising 80 mg of (+) cicletanine and 120 mg of ( ⁇ ) cicletanine is administered via an oral route once daily, to patients with asthma or COPD or pulmonary fibrosis.
• Cicletanine is administered alone or in combination with other classes of drugs as discussed above.
• pulmonary function is improved, systemic blood pressure remains within acceptable limits, and in addition one or more of the following parameters is improved: FEV1, O2 saturation, walking distance, prostacyclin/thromboxane ratio, and NYHA functional class score. Metabolic parameters remain unchanged or improved. Such improvements remain above baseline for at least 3 months.
• Such a formulation has a less prominent diuretic effect and is most appropriate for patients experiencing intermediate fluid overload.
• a cicletanine formulation comprising 60 mg of (+) cicletanine and 140 mg of ( ⁇ ) cicletanine is administered via an oral route once daily, to patients with asthma or COPD or pulmonary fibrosis.
• Cicletanine is administered alone or in combination with other classes of drugs as discussed above.
• pulmonary function is improved, systemic blood pressure remains within acceptable limits, and in addition one or more of the following parameters is improved: FEV1, O2 saturation, walking distance, prostacyclin/thromboxane ratio, and NYHA functional class score. Metabolic parameters remain unchanged or improved. Such improvements remain above baseline for at least 3 months.
• Such a formulation has a less prominent diuretic effect and is most appropriate for patients experiencing intermediate fluid overload.
• a cicletanine formulation comprising 40 mg of (+) cicletanine and 160 mg of ( ⁇ ) cicletanine is administered via an oral route once daily, to patients with asthma or COPD or pulmonary fibrosis.
• Cicletanine is administered alone or in combination with other classes of drugs as discussed above.
• pulmonary function are improved, systemic blood pressure remains within acceptable limits, and in addition one or more of the following parameters is improved: FEV1, O2 saturation, walking distance, prostacyclin/thromboxane ratio, and NYHA functional class score. Metabolic parameters remain unchanged or improved. Such improvements remain above baseline for at least 3 months.
• Such a formulation has a mild diuretic effect and strong nitric oxide effect and is most appropriate for patients experiencing modest fluid overload.
• a cicletanine formulation comprising 20 mg of (+) cicletanine and 180 mg of ( ⁇ ) cicletanine is administered via an oral route once daily, to patients with asthma or COPD or pulmonary fibrosis.
• Cicletanine is administered alone or in combination with other classes of drugs as discussed above.
• pulmonary function is improved, systemic blood pressure remains within acceptable limits, and in addition one or more of the following parameters improved: FEV1, O2 saturation, walking distance, prostacyclin/thromboxane ratio, and NYHA functional class score. Metabolic parameters remain unchanged or improved. Such improvements remain above baseline for at least 3 months.
• Such a formulation has a mild diuretic effect and strong nitric oxide effects and is most appropriate for patients experiencing modest fluid overload or no fluid overload.
• a cicletanine formulation comprising 200 mg of ( ⁇ ) cicletanine is administered via an oral route once daily, to patients with asthma or COPD or pulmonary fibrosis.
• Cicletanine is administered alone or in combination with other classes of drugs as discussed above.
• pulmonary function is improved, systemic blood pressure remains within acceptable limits, and in addition one or more of the following parameters is improved: FEV1, O2 saturation, walking distance, prostacyclin/thromboxane ratio, and NYHA functional class score. Metabolic parameters remain unchanged or improved. Such improvements remain above baseline for at least 3 months.
• This formulation has little or no diuretic effect, and maximal nitric oxide effect, and is best suited to patients with no fluid overload.
• a cicletanine formulation comprising 200 mg of (+) cicletanine is administered via an oral route once daily, to patients with heart failure or cor pulmonale.
• Cicletanine is administered alone or in combination with other classes of drugs as discussed above.
• cardiac function is improved or stabilized, systemic blood pressure remains within acceptable limits, and in addition one or more of the following parameters is improved: Natriuretic peptide levels, cardiac output, walking distance, and NYHA functional class score. Metabolic parameters remain unchanged or improved. Such improvements remain above baseline for at least 3 months.
• Such a formulation has a prominent diuretic effect and is most appropriate for patients experiencing substantial fluid overload.
• a cicletanine formulation comprising 180 mg of (+) cicletanine and 20 mg of ( ⁇ ) cicletanine is administered via an oral route once daily, to patients with heart failure or cor pulmonale.
• Cicletanine is administered alone or in combination with other classes of drugs as discussed above.
• systemic blood pressure remains within acceptable limits, and in addition one or more of the following parameters is improved: Natriuretic peptide levels, cardiac output, walking distance, and NYHA functional class score. Metabolic parameters remain unchanged or improved. Such improvements remain above baseline for at least 3 months.
• Such a formulation has a prominent diuretic effect and is most appropriate for patients experiencing substantial fluid overload.
• a cicletanine formulation comprising 160 mg of (+) cicletanine and 40 mg of ( ⁇ ) cicletanine is administered via an oral route once daily, to patients with heart failure or cor pulmonale.
• Cicletanine is administered alone or in combination with other classes of drugs as discussed above.
• cardiac function is improved, systemic blood pressure remains within acceptable limits, and in addition one or more of the following parameters is improved: Natriuretic peptide levels, cardiac output, walking distance, and NYHA functional class score. Metabolic parameters remain unchanged or improved. Such improvements remain above baseline for at least 3 months.
• Such a formulation has a prominent diuretic effect and is most appropriate for patients experiencing substantial fluid overload.
• a cicletanine formulation comprising 140 mg of (+) cicletanine and 60 mg of ( ⁇ ) cicletanine is administered via an oral route once daily, to patients with heart failure or cor pulmonary.
• Cicletanine is administered alone or in combination with other classes of drugs as discussed above.
• cardiac function is improved, systemic blood pressure remains within acceptable limits, and in addition one or more of the following parameters is improved: Natriuretic peptide levels, cardiac output, walking distance, and NYHA functional class score. Metabolic parameters remain unchanged or improved. Such improvements remain above baseline for at least 3 months.
• Such a formulation has a less prominent diuretic effect and is most appropriate for patients experiencing midrange fluid overload.
• a cicletanine formulation comprising 120 mg of (+) cicletanine and 80 mg of ( ⁇ ) cicletanine is administered via an oral route once daily, to patients with heart failure or cor pulmonale.
• Cicletanine is administered alone or in combination with other classes of drugs as discussed above.
• cardiac function is improved, systemic blood pressure remains within acceptable limits, and in addition one or more of the following parameters is improved: Natriuretic peptide levels, cardiac output, walking distance, and NYHA functional class score. Metabolic parameters remain unchanged or improved. Such improvements remain above baseline for at least 3 months.
• Such a formulation has a less prominent diuretic effect and is most appropriate for patients experiencing intermediate fluid overload.
• a cicletanine formulation comprising 100 mg of (+) cicletanine and 100 mg of ( ⁇ ) cicletanine is administered via an oral route once daily, to patients with heart failure or cor pulmonale.
• Cicletanine is administered alone or in combination with other classes of drugs as discussed above.
• cardiac function is improved or stabilized, blood pressure remains within acceptable limits, and in addition one or more of the following parameters is improved: Natriuretic peptide levels, cardiac output, walking distance, and NYHA functional class score. Metabolic parameters remain unchanged or improved. Such improvements remain above baseline for at least 3 months.
• Such a formulation has a mid range diuretic effect and is most appropriate for patients experiencing intermediate fluid overload.
• a cicletanine formulation comprising 80 mg of (+) cicletanine and 120 mg of ( ⁇ ) cicletanine is administered via an oral route once daily, to patients with heart failure or cor pulmonale.
• Cicletanine is administered alone or in combination with other classes of drugs as discussed above.
• cardiac function is improved, systemic blood pressure remains within acceptable limits, and in addition one or more of the following parameters is improved: Natriuretic peptide levels, cardiac output, walking distance, and NYHA functional class score. Metabolic parameters remain unchanged or improved. Such improvements remain above baseline for at least 3 months.
• Such a formulation has a less prominent diuretic effect and is most appropriate for patients experiencing intermediate fluid overload.
• a cicletanine formulation comprising 60 mg of (+) cicletanine and 140 mg of ( ⁇ ) cicletanine is administered via an oral route once daily, to patients with heart failure or cor pulmonale.
• Cicletanine is administered alone or in combination with other classes of drugs as discussed above.
• cardiac function is improved, systemic blood pressure remains within acceptable limits, and in addition one or more of the following parameters is improved: Natriuretic peptide levels, cardiac output, walking distance, and NYHA functional class score. Metabolic parameters remain unchanged or improved. Such improvements remain above baseline for at least 3 months.
• Such a formulation has a less prominent diuretic effect and is most appropriate for patients experiencing intermediate fluid overload.
• a cicletanine formulation comprising 40 mg of (+) cicletanine and 160 mg of ( ⁇ ) cicletanine is administered via an oral route once daily, to patients with heart failure or cor pulmonale.
• Cicletanine is administered alone or in combination with other classes of drugs as discussed above.
• cardiac function is improved, systemic blood pressure remains within acceptable limits, and in addition one or more of the following parameters is improved: Natriuretic peptide levels, cardiac output, walking distance, and NYHA functional class score. Metabolic parameters remain unchanged or improved. Such improvements remain above baseline for at least 3 months.
• Such a formulation has a mild diuretic effect and strong nitric oxide effect and is most appropriate for patients experiencing modest fluid overload.
• a cicletanine formulation comprising 20 mg of (+) cicletanine and 180 mg of ( ⁇ ) cicletanine is administered via an oral route once daily, to patients with heart failure or cor pulmonale.
• Cicletanine is administered alone or in combination with other classes of drugs as discussed above.
• cardiac function is improved, systemic blood pressure remains within acceptable limits, and in addition one or more of the following parameters is improved: Natriuretic peptide levels, cardiac output, walking distance, and NYHA functional class score. Metabolic parameters remain unchanged or improved. Such improvements remain above baseline for at least 3 months.
• Such a formulation has a mild diuretic effect and strong nitric oxide effects and is most appropriate for patients experiencing modest fluid overload or no fluid overload.
• a cicletanine formulation comprising 200 mg of ( ⁇ ) cicletanine is administered via an oral route once daily, to patients with heart failure or cor pulmonale.
• Cicletanine is administered alone or in combination with other classes of drugs as discussed above.
• cardiac function is improved, systemic blood pressure remains within acceptable limits, and in addition one or more of the following parameters is improved: Natriuretic peptide levels, cardiac output, walking distance, and NYHA functional class score. Metabolic parameters remain unchanged or improved. Such improvements remain above baseline for at least 3 months.
• This formulation has little or no diuretic effect, and maximal nitric oxide effect, and is best suited to patients with no fluid overload.
• a non-racemic combination drug is formulated into a pill, capsule or other dosage form of mixed composition comprising approximately 90 mg of the (+) enantiomer of Cicletanine and is combined with 10 mg of the ( ⁇ ) enantiomer of Cicletanine and is administered orally, once a day, to subjects suffering from pulmonary hypertension.
• the nonracemic formulated drug is administered, alone or in combination with drugs from other classes, either as a first-line drug or as a drug given in addition to or as a replacement for a previous/current drug given for pulmonary hypertension.
• pulmonary blood pressure favorably falls and a positive effect upon metabolic parameters (in particular, blood glucose levels, glucose tolerance, blood triglyceride levels, blood cholesterol [total, LDL and Ha] levels) will either be positive or neutral, as compared to controls.
• metabolic parameters in particular, blood glucose levels, glucose tolerance, blood triglyceride levels, blood cholesterol [total, LDL and Ha] levels
• non-racemic drug formulation has a predominantly-diuretic effect, while having some pulmonary vasorelaxant and organ-protective effects. Additionally, the potassium-lowering effect and the effect of this drug upon lipids and cholesterol is healthier and less pronounced than that of the thiazide-type diuretics.
• a non-racemic combination drug is formulated into a pill, capsule or other dosage form of mixed composition of approximately 80 mg of the (+) enantiomer of Cicletanine and is combined with 20 mg of the ( ⁇ ) enantiomer of Cicletanine and is administered orally, once a day, to subjects suffering symptoms from one or more of the following descriptions: pulmonary hypertension.
• the formulated drug is administered either as a first-line drug or as a drug given in addition to, or as a replacement for a previous/current drug given for pulmonary hypertension.
• pulmonary blood pressure falls favorably and effects upon metabolic parameters (in particular, blood glucose levels, glucose tolerance, blood triglyceride levels, blood cholesterol [total, LDL and HDL] levels) are positive or remain neutral to minimal.
• non-racemic drug formulation has a predominantly-diuretic effect, while having some pulmonary vasorelaxant and organ-protective effects. Additionally, the potassium-lowering effect and the effect of this drug upon lipids and cholesterol are healthier and less pronounced than that of the thiazide-type diuretics.
• a non-racemic combination drug is formulated into a pill, capsule or other dosage form of mixed composition of approximately 70 mg of the (+) enantiomer of Cicletanine combined with 30 mg of the ( ⁇ ) enantiomer of Cicletanine and is administered orally once a day to subjects suffering symptoms from one or more of the following descriptions: pulmonary hypertension, either alone or combined with drugs from other classes or pulmonary hypertension in the presence of mildly or moderately-elevated triglycerides, cholesterol or blood glucose, but not in the presence of actual metabolic syndrome.
• the nonracemic formulated drug is administered, alone or in combination with drugs from other classes, either as a first-line drug or as a drug given in addition to or as a replacement for a previous/current drug given for pulmonary hypertension.
• pulmonary blood pressure falls favorably, and effects upon metabolic parameters (in particular, blood glucose levels, glucose tolerance, blood triglyceride levels, blood cholesterol [total, LDL and HDL] levels) are positive or remain neutral to minimal.
• the potassium-lowering effect and the effect of this drug upon lipids and cholesterol are healthier and less pronounced than that of the thiazide-type diuretics.
• a non-racemic combination drug is formulated into a pill, capsule or other dosage form of mixed composition of approximately 60 mg of the (+) enantiomer of Cicletanine combined with 40 mg of the ( ⁇ ) enantiomer of Cicletanine and is administered orally, once a day, to subjects suffering symptoms from one or more of the following descriptions: pulmonary hypertension in the presence of mildly or moderately-elevated triglycerides, cholesterol, or blood glucose both in and out of the presence of actual metabolic syndrome.
• the drug is administered either as a first-line drug or as a drug given in addition to, or as a replacement for a previous/current drug given for pulmonary hypertension.
• pulmonary blood pressure falls favorably and effects upon metabolic parameters (in particular, blood glucose levels, glucose tolerance, blood triglyceride levels, blood cholesterol [total, LDL and HDL] levels) are positive or remain neutral to minimal.
• a non-racemic combination drug is formulated into a pill, capsule or other dosage form of mixed composition of approximately 40 mg of the (+) enantiomer of Cicletanine combined with 60 mg of the ( ⁇ ) enantiomer of Cicletanine and is administered orally, once a day, to subjects suffering symptoms from one or more of the following descriptions: uncomplicated pulmonary hypertension, either alone or combined with drugs from other classes; hypertension in the presence of mildly or moderately-elevated triglycerides, cholesterol or blood glucose; pulmonary hypertension in the presence of diabetes or metabolic syndrome.
• the drug is administered either as a first-line drug or as a drug given in addition to, or as a replacement for a previous/current drug given for pulmonary hypertension or other pulmonary diseases or complications thereof.
• pulmonary blood pressure falls favorably, and effects upon metabolic parameters (in particular, blood glucose levels, glucose tolerance, blood triglyceride levels, blood cholesterol [total, LDL and HDL] levels) are positive or remain neutral to minimal.
• non-racemic drug formulation has a diuretic effect, as well as pulmonary vasorelaxant and organ-protective effects.
• the pulmonary vasorelaxant effects are more pronounced than the other effects.
• the potassium-lowering effect and the effect of this drug upon lipids and cholesterol is healthier and less pronounced than that of the thiazide-type diuretics.
• a non-racemic combination drug is formulated into a pill, capsule or other dosage form of mixed composition of approximately 30 mg of the (+) enantiomer of Cicletanine combined with 70 mg of the ( ⁇ ) enantiomer of Cicletanine and is administered orally, once a day, to subjects suffering symptoms from one or more of the following descriptions: uncomplicated pulmonary hypertension, either alone or combined with drugs from other classes; hypertension in the presence of mildly or moderately-elevated triglycerides, cholesterol or blood glucose; pulmonary hypertension in the presence of diabetes or metabolic syndrome.
• the drug is administered either as a first-line drug or as a drug given in addition to, or as a replacement for a previous/current drug given for pulmonary hypertension, other pulmonary diseases, or complications thereof.
• pulmonary blood pressure falls favorably and effects upon metabolic parameters (in particular, blood glucose levels, glucose tolerance, blood triglyceride levels, blood cholesterol [total, LDL and HDL] levels) are positive or remain neutral to minimal.
• non-racemic drug formulation has a diuretic effect, as well as pulmonary vasorelaxant and organ-protective effects.
• the vasorelaxant and organ protective effects are more pronounced than the other effects.
• the potassium-lowering effect and the effect of this drug upon lipids and cholesterol is healthier and less pronounced than that of the thiazide-type diuretics.
• a non-racemic combination drug is formulated into a pill, capsule or other dosage form of mixed composition of approximately 20 mg of the (+) enantiomer of Cicletanine combined with. 80 mg of the ( ⁇ ) enantiomer of Cicletanine and is administered orally, once a day, to subjects suffering symptoms from one or more of the following descriptions: uncomplicated pulmonary hypertension, either alone or combined with drugs from other classes; hypertension in the presence of mildly or moderately-elevated triglycerides, cholesterol or blood glucose.
• the drug is administered either as a first-line drug or as a drug given in addition to, or as a replacement for a previous/current drug given for pulmonary hypertension, other pulmonary diseases, or complications thereof.
• pulmonary blood pressure falls favorably and effects upon metabolic parameters (in particular, blood glucose levels, glucose tolerance, blood triglyceride levels, blood cholesterol [total, LDL and HDL] levels) are positive or remain neutral to minimal.
• the non-racemic drug formulation above has a diuretic effect, as well as vasorelaxant and organ-protective effects.
• the vasorelaxant and organ protective effects are more pronounced than the diuretic effect.
• the potassium-lowering effect and the effect of this drug upon lipids and cholesterol are healthier and less pronounced than that of the thiazide-type diuretics.
• a non-racemic combination drug is formulated into a pill, capsule or other dosage form of mixed composition of approximately 10 mg of the (+) enantiomer of Cicletanine combined with 90 mg of the ( ⁇ ) enantiomer of Cicletanine and is administered orally, once a day, to subjects suffering symptoms from one or more of the following descriptions: pulmonary hypertension, either alone or combined with drugs from other classes; pulmonary hypertension in the presence of mildly or moderately-elevated triglycerides, cholesterol or blood glucose; pulmonary hypertension in the presence of diabetes or metabolic syndrome.
• the drug is administered either as a first-line drug or as a drug given in addition to, or as a replacement for a previous/current drug given for pulmonary hypertension, other pulmonary diseases, or complications thereof.
• pulmonary blood pressure falls favorably and effects upon metabolic parameters (in particular, blood glucose levels, glucose tolerance, blood triglyceride levels, blood cholesterol [total, LDL and HDL] levels) are positive or remain neutral to minimal.
• non-racemic drug formulation has a diuretic effect, as well as pulmonary vasorelaxant and organ-protective effects.
• the pulmonary vasorelaxant and organ protective effects are more pronounced than the diuretic effect.
• the potassium-lowering effect and the effect of this drug upon lipids and cholesterol are healthier and less pronounced than that of the thiazide-type diuretics.
• the various cicletanine compositions may be the sole therapeutic agent of the formulation, in other embodiments, a second agent or agents may be included along with the cicletanine composition.
• “Second agent”, as used herein, refers to any agent other than the cicletanine compositions; “second agent”, as such is a generic term that may include a plurality of agents that are members of this non-cicletanine class.
• Such second agents may be, by themselves, effective agents for increasing prostacyclin, antagonizing endothelin activity, inhibiting phosphodiesterase activity, inhibiting histaminergic activity, inhibition of calcium-channel activity, enhancing cGMP activity, acting as a Nitrogen donor or NO enhancer, and/or treating any complications associated with pulmonary diseases.
• the range of diseases and associated complications or sequalae that receive therapeutic benefit from formulations consisting only of cicletanine compositions are understood to be the same as those that receive benefit from formulations that include both cicletanine, of varying enantiomeric composition, and a second therapeutic agent.
• an oral formulation comprising a therapeutically effective amount of cicletanine alone or in combination with a second agent such that the overall formulation improves pulmonary hemodynamics without inappropriately lowering systemic blood pressure.
• Cicletanine might be favorable in this regard because it tends not to lower systemic blood pressure in patients who do not have systemic hypertension. This phenomenon of not lowering systemic blood pressure in systemic normotensives has been observed by the inventors to be more marked than that of other blood-pressure lowering agents.
• cicletanine correcting the root of endogenous deficits (e.g., reversing the decoupling endothelial nitric oxide synthase [eNOS]) rather than over-riding a dysfunctional biochemical cascade by endeavoring to counterbalance downstream phenomena (such downstream counterbalancing is what is done by the major classes of vasorelaxant antihypertensives: ACE inhibitors, angiotensin receptor blockers, calcium-channel blockers and beta blockers).
• ACE inhibitors angiotensin receptor blockers
• calcium-channel blockers and beta blockers
• a method for treating and/or preventing a condition or complication associated with pulmonary diseases such as asthma or other chronic obstructive pulmonary diseases.
• Cicletanine is thought by the inventors to be of particular interest here, because the inventors have observed that cicletanine, in addition to enhancing systemic prostacyclin and enhancing the coupling of endothelial nitric oxide synthase (eNOS), will also inhibit the excessive histaminergic activity associated with asthma or COPD.
• eNOS endothelial nitric oxide synthase
• This antihistaminergic activity is proposed to be associated with the ( ⁇ ) stereoisomer, but not the (+) stereoisomer of cicletanine.
• the method comprises administering cicletanine (in racemic, non-racemic or pure stereoisomeric forms) via aerosol delivery to the lungs and administering a second pulmonary hypertension agent that acts either as a calcium-channel blocker, phosphodiesterase in inhibitor, prostacyclin analogue or endothelin antagonist, cGMP enhancer, or Nitrogen donor.
• a second pulmonary hypertension agent that acts either as a calcium-channel blocker, phosphodiesterase in inhibitor, prostacyclin analogue or endothelin antagonist, cGMP enhancer, or Nitrogen donor.
• the therapeutically effective amount of the cicletanine is sufficient to mitigate a side effect of the second agent.
• the amounts of the cicletanine and second agents are sufficient to produce a synergistic antihypertensive effect.
• the addition of cicletanine enhances the duration of action of the second agent or reduces the development of tolerance to the second agent.
• the use of cicletanine allows for a lower dosage of a second agent treating pulmonary hypertension, thereby decreasing the frequency or severity of the adverse events associated with that second agent.
• Embodiments of the present invention may make use of cicletanine as an inducer of prostacyclin, although cicletanine may operate through other mechanisms as well, including diuresis.
• Cicletanine in the course of standard synthesis procedures, naturally occurs as a racemic mixture of equal proportions of a positive (+) and a negative ( ⁇ ) enantiomer, however, embodiments of the present invention include formulations that consist purely of either the positive (+) or negative ( ⁇ ) enantiomer, as well as formulations with non-racemic mixtures that may vary in relative proportions, ranging from, for example a formulation with a proportion of about 99% (+) enantiomer: about 1% ( ⁇ ) enantiomer to a formulation with a proportion of about 1% (+) enantiomer: about 99% ( ⁇ ) enantiomer.
• the combination therapies may comprise fixed doses (of each component), in single-tablet form, single-capsule form, or other combined-dosage forms.
• combination of therapies within a single tablet is meant to simplify treatment regimens, and thereby support patient compliance.
• doses of the combined agents relative to each other are fixed, based on supporting an appropriate level of simplicity for treatment regimens. The establishment of doses appropriately that are fixed relative to each other still allows for variation in total dosage.
• Combination therapy in general, supports appropriate-level dosing in that it allows the application of doses of individual agents lower than those that elicit the unwanted side effects that may occur at higher dose levels.
• synergistic therapeutic effects may occur. Synergistic effects, by their nature, are not commonly predictable, based solely on an understanding of the respective mechanisms of the combined individual agents.
• a therapeutic embodiment of the present invention comprises a prostacyclin, or more particularly, an agonist or an inducer thereof (particularly via upregulation of nitric oxide) such as a composition of cicletanine, in combination with (1) prostacyclin-analogue agents, such as epoprostenol, iloprost, and treprostinil; (2) endothelin antagonists, such as bosentan; (3) PDE inhibitors such a sildenafil; (4) calcium-channel blockers such as nifedipine, amlodipine and nicardipine; (5) a Nitrogen donor or enhancer, such as SNP, and (6) an inducer or enhancer of cGMP, such as ANP.
• a prostacyclin or more particularly, an agonist or an inducer thereof (particularly via upregulation of nitric oxide) such as a composition of cicletanine, in combination with (1) prostacyclin-analogue agents, such as epoprostenol, i
• the combination may be formulated in accordance with the teachings herein to provide a clinical benefit that goes beyond the beneficial effects produced by either drug alone.
• Such an enhanced clinical benefit may be related to distinct mechanisms of action and/or a synergistic interaction of the drugs.
• aspects of embodiments of the present invention are applicable in the treatment of PH and related disorders for children and adults.

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